Research Topics
Species | Michael B FisherSummaryAffiliation: Boehringer Ingelheim Publications
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Detail Information
Publications
In vivo use of the P450 inactivator 1-aminobenzotriazole in the rat: varied dosing route to elucidate gut and liver contributions to first-pass and systemic clearanceTimothy J Strelevitz
Pfizer Inc, PGRD, Pharmacokinetics, Dynamics, and Metabolism, Eastern Point Road, Groton, CT 06340, USA
J Pharm Sci 95:1334-41. 2006..This method should have utility in drug discovery for the identification of factors limiting oral bioavailability...
Prevention of organ allograft rejection by a specific Janus kinase 3 inhibitorPaul S Changelian
Immunology Group, Department of Antibacterials and Immunology, Pfizer Global Researchand Development, Groton, CT 06340, USA
Science 302:875-8. 2003..On the basis of these preclinical results, we believe JAK3 blockade by CP-690,550 has potential for therapeutically desirable immunosuppression in human organ transplantation and in other clinical settings...
Altered AZT (3'-azido-3'-deoxythymidine) glucuronidation kinetics in liver microsomes as an explanation for underprediction of in vivo clearance: comparison to hepatocytes and effect of incubation environmentJuntyma J Engtrakul
Pharmacokinetics, Dynamics, and Metabolism, Pfizer Global Research and Development, Groton, CT 06340, USA
Drug Metab Dispos 33:1621-7. 2005....
A streamlined method to predict hepatic clearance using human liver microsomes in the presence of human plasmaSara M Skaggs
Pfizer Global Research and Development, Pharmacokinetics, Dynamics, and Metabolism Pfizer, Inc. Groton, CT 06340, USA
J Pharmacol Toxicol Methods 53:284-90. 2006....
The complexities inherent in attempts to decrease drug clearance by blocking sites of CYP-mediated metabolismMichael B Fisher
Boehringer Ingelheim Pharmaceuticals Inc, 900 Ridgebury Road, Ridgefield, CT 06877, USA
Curr Opin Drug Discov Devel 9:101-9. 2006..The concepts and evidence behind this phenomenon as it relates to complexities in blocking metabolic clearance are presented herein...
Time-dependent inhibition and estimation of CYP3A clinical pharmacokinetic drug-drug interactions using plated human cell systemsDaniel R Albaugh
Boehringer Ingelheim Pharmaceuticals Inc, Medicinal Chemistry Drug Metabolism and Pharmacokinetics, 175 Briar Ridge Road, R and D 10574, Ridgefield, CT 06877, USA
Drug Metab Dispos 40:1336-44. 2012..Overall, results from these studies suggest that in vitro inactivation parameters generated from plated cell systems may be a practical approach for identifying time-dependent inhibitors and for estimating the magnitude of clinical DDIs...
Characterization of aldehyde oxidase enzyme activity in cryopreserved human hepatocytesJ Matthew Hutzler
Boehringer Ingelheim Pharmaceuticals Inc, Translational Research Drug Metabolism and Pharmacokinetics, 175 Briar Ridge Road, R and D 10578, Ridgefield, CT 06877, USA
Drug Metab Dispos 40:267-75. 2012..These data taken together suggest that the use of cryopreserved hepatocytes may be a practical approach for assessing AO-mediated metabolism in discovery and potentially useful for predicting hepatic clearance of AO substrates...
The role of the intestine in drug metabolism and pharmacokinetics: an industry perspectiveMichael B Fisher
Cara Therapeutics, Tarrytown, NY 10591, USA
Curr Drug Metab 8:694-9. 2007..The opportunity exists to increase the examination of intestinal metabolism of drugs and drug candidates in industry...
Recent advances in high throughput screening for ADME propertiesTimothy J Carlson
Amgen Inc, 1120 Veterans Boulevard, South San Francisco, CA 94080, USA
Comb Chem High Throughput Screen 11:258-64. 2008..Future advances will further improve the ability to make decisions on molecules earlier in drug discovery...
